| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55908034-55908304 | Rare:44 | ||||
| chrX:56291883-56291998 | Rare:20 | ||||
| chrX:56764328-56764835 | Common:1; Rare:141 | ||||
| chrX:56803064-56803721 | Common:4; Rare:152 | ||||
| chrX:63350645-63350811 | Common:1; Rare:33 | ||||
| chrX:63560940-63561175 | Rare:59 | ||||
| chrX:64204838-64204988 | Rare:42 | ||||
| chrX:64975290-64975860 | Common:1; Rare:81 | ||||
| chrX:65136448-65136848 | Common:1; Rare:98 | ||||
| chrX:65920669-65921162 | Common:1; Rare:148 | ||||
| chrX:67546078-67546478 | Common:1; Rare:153; Clinvar:3 | ||||
| chrX:67546474-67547400 | Common:10; Rare:220; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chrX:68332330-68332766 | Common:2; Rare:75 | ||||
| chrX:68829738-68830138 | Common:1; Rare:85 | ||||
| chrX:68846501-68847041 | Common:4; Rare:133 |